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2-Azido-1-(4-morpholin-4-ylphenyl)ethanone | 864528-25-6

中文名称
——
中文别名
——
英文名称
2-Azido-1-(4-morpholin-4-ylphenyl)ethanone
英文别名
——
2-Azido-1-(4-morpholin-4-ylphenyl)ethanone化学式
CAS
864528-25-6
化学式
C12H14N4O2
mdl
——
分子量
246.269
InChiKey
UAPCVGQHINIRBV-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    43.9
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    2-Anilino-4-aryl-1,3-thiazole inhibitors of valosin-containing protein (VCP or p97)
    摘要:
    Valosin-containing protein (VCP; also known as p97) is a member of the AAA ATPase family with a central role in the ubiquitin-degradation of misfolded proteins. VCP also exhibits antiapoptotic function and metastasis via activation of nuclear factor kappa-B signaling pathway. We have discovered that 2-anilino-4-aryl-1,3-thiazoles are potent drug-like inhibitors of this enzyme. The identified compounds show low nanomolar VCP potency, demonstrate SAR trends, and show activity in a mechanism based cellular assay. This series of compounds represents the first steps towards a novel, small molecule VCP inhibitor as a cancer therapeutic. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.01.058
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文献信息

  • Macrocyclic Compounds And Methods Of Making And Using The Same
    申请人:Farmer J. Jay
    公开号:US20080045585A1
    公开(公告)日:2008-02-21
    The present invention provides macrocyclic compounds useful as therapeutic agents. More particularly, these compounds are useful as anti-infective, anti-proliferative, anti-inflammatory, and prokinetic agents.
    本发明提供了一种用作治疗剂的大环化合物。更具体地说,这些化合物可用作抗感染、抗增殖、抗炎和促动力剂。
  • MACROCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING THE SAME
    申请人:Farmer Jay J.
    公开号:US20120252747A1
    公开(公告)日:2012-10-04
    The present invention provides macrocyclic compounds useful as therapeutic agents of the formula: or a pharmaceutically acceptable salt, ester, N-oxide, or prodrug thereof, wherein T, R 1 , R 2 , R 3 , D, E, F, and G are as defined herein. More particularly, these compounds are useful as anti-infective, antiproliferative, anti-inflammatory and prokinetic agents.
    本发明提供了通式为的大环化合物,可用作治疗剂,或其药学上可接受的盐、酯、N-氧化物或前药,其中T、R1、R2、R3、D、E、F和G如本文所定义。更具体地,这些化合物可用作抗感染、抗增殖、抗炎和促动力剂。
  • US8202843B2
    申请人:——
    公开号:US8202843B2
    公开(公告)日:2012-06-19
  • US8841263B2
    申请人:——
    公开号:US8841263B2
    公开(公告)日:2014-09-23
  • 2-Anilino-4-aryl-1,3-thiazole inhibitors of valosin-containing protein (VCP or p97)
    作者:Matthew G. Bursavich、Daniel P. Parker、J. Adam Willardsen、Zhong-Hua Gao、Thaylon Davis、Kirill Ostanin、Rosann Robinson、Ashley Peterson、Daniel M. Cimbora、Ju-Fen Zhu、Burt Richards
    DOI:10.1016/j.bmcl.2010.01.058
    日期:2010.3
    Valosin-containing protein (VCP; also known as p97) is a member of the AAA ATPase family with a central role in the ubiquitin-degradation of misfolded proteins. VCP also exhibits antiapoptotic function and metastasis via activation of nuclear factor kappa-B signaling pathway. We have discovered that 2-anilino-4-aryl-1,3-thiazoles are potent drug-like inhibitors of this enzyme. The identified compounds show low nanomolar VCP potency, demonstrate SAR trends, and show activity in a mechanism based cellular assay. This series of compounds represents the first steps towards a novel, small molecule VCP inhibitor as a cancer therapeutic. (C) 2010 Elsevier Ltd. All rights reserved.
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